Canonical Allele Identifier: PA2826635844
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89259
ClinVar RCV Id: RCV000568729 RCV000524133 RCV000662512 RCV001582560 RCV003997072 RCV003466941
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Phe424Tyr
CA009822
NM_001281494.2:c.1271T>A